<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Klid S</submitter><funding>Instituto de Salud Carlos III</funding><funding>Spanish Ministry of Science and Innovation</funding><funding>Miguel Servet tenure-track program</funding><funding>Agency for Administration of University and Research</funding><funding>Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas</funding><pagination>2486</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9917010</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(3)</volume><pubmed_abstract>Dyslipidemia in gestational diabetes has been associated with worse perinatal outcomes. The ANGPTL3-4-8 axis regulates lipid metabolism, especially in the transition from fasting to feeding. In this study, we evaluated the response of ANGPTL3, 4, and 8 after the intake of a mixed meal in women with normal glucose tolerance and gestational diabetes, and we assessed their gene expressions in different placental locations. Regarding the circulating levels of ANGPTL3, 4, and 8, we observed an absence of ANGPTL4 response after the intake of the meal in the GDM group compared to its presence in the control group. At the placental level, we observed a glucose tolerance-dependent expression pattern of &lt;i>ANGPTL3&lt;/i> between the two placental sides. When we compared the GDM pregnancies with the con</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>The ANGPTL3-4-8 Axis in Normal Gestation and in Gestational Diabetes, and Its Potential Involvement in Fetal Growth.</pubmed_title><pmcid>PMC9917010</pmcid><funding_grant_id>RTI2018-093919-B-100</funding_grant_id><funding_grant_id>CB07708/0012</funding_grant_id><funding_grant_id>2020FI_B 00980</funding_grant_id><funding_grant_id>PID2021-122480OB-100</funding_grant_id><funding_grant_id>PI 18/00516</funding_grant_id><funding_grant_id>PI 20/00338</funding_grant_id><funding_grant_id>PI 15/01562</funding_grant_id><funding_grant_id>CPII16/00008</funding_grant_id><funding_grant_id>CP10/00438</funding_grant_id><funding_grant_id>PI 21/01479</funding_grant_id><pubmed_authors>Jareno C</pubmed_authors><pubmed_authors>Klid S</pubmed_authors><pubmed_authors>Algaba-Chueca F</pubmed_authors><pubmed_authors>Ingles-Puig M</pubmed_authors><pubmed_authors>Vendrell J</pubmed_authors><pubmed_authors>Maymo-Masip E</pubmed_authors><pubmed_authors>Fernandez-Veledo S</pubmed_authors><pubmed_authors>Madeira A</pubmed_authors><pubmed_authors>Ballesteros M</pubmed_authors><pubmed_authors>Guarque A</pubmed_authors><pubmed_authors>Megia A</pubmed_authors></additional><is_claimable>false</is_claimable><name>The ANGPTL3-4-8 Axis in Normal Gestation and in Gestational Diabetes, and Its Potential Involvement in Fetal Growth.</name><description>Dyslipidemia in gestational diabetes has been associated with worse perinatal outcomes. The ANGPTL3-4-8 axis regulates lipid metabolism, especially in the transition from fasting to feeding. In this study, we evaluated the response of ANGPTL3, 4, and 8 after the intake of a mixed meal in women with normal glucose tolerance and gestational diabetes, and we assessed their gene expressions in different placental locations. Regarding the circulating levels of ANGPTL3, 4, and 8, we observed an absence of ANGPTL4 response after the intake of the meal in the GDM group compared to its presence in the control group. At the placental level, we observed a glucose tolerance-dependent expression pattern of &lt;i>ANGPTL3&lt;/i> between the two placental sides. When we compared the GDM pregnancies with the con</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-25T19:23:53.046Z</modification><creation>2025-04-06T07:57:48.176Z</creation></dates><accession>S-EPMC9917010</accession><cross_references><pubmed>36768809</pubmed><doi>10.3390/ijms24032486</doi></cross_references></HashMap>